Search results for "paroxysmal dyskinesia"

The MalaCard for "paroxysmal dyskinesia" has been retired.
Searching MalaCards for entries containing "paroxysmal dyskinesia"

224 hits were found for 'paroxysmal dyskinesia'

# Family MCID Name MIFTS Score
1
FML185 Familial Paroxysmal Kinesigenic Dyskinesia 21 7.801
2
c FML186 Familial Paroxysmal Nonkinesigenic Dyskinesia 15 6.207
3
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 5.794
4
GNR006 Generalized Epilepsy and Paroxysmal Dyskinesia 19 5.742
5
P PRX004 Paroxysmal Nonkinesigenic Dyskinesia 31 5.226
6
P EPS030 Episodic Kinesigenic Dyskinesia 1 26 4.180
7
c PRX024 Paroxysmal Nonkinesigenic Dyskinesia 2 11 4.043
8
GLT019 Glut1 Deficiency Syndrome 2 32 3.594
9
PRX022 Paroxysmal Choreoathetosis 23 3.078
10
PRX086 Paroxysmal Exertion-Induced Dyskinesia 11 2.938
11
P PRM011 Primary Ciliary Dyskinesia 56 0.505
12
P DYS154 Dystonia 62 0.265
13
MVM001 Movement Disease 45 0.245
14
ALR002 Al-Raqad Syndrome 36 0.240
15
P EPL164 Epilepsy 60 0.204
16
DRG016 Drug Induced Dyskinesia 19 0.201
17
P ENC018 Encephalopathy 59 0.195
18
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.192
19
c CNT035 Central Nervous System Disease 60 0.170
20
P NRV007 Nervous System Disease 71 0.161
21
BSL008 Basal Ganglia Disease 40 0.155
22
c CNG401 Congenital Heart Disease 67 0.150
23
VND001 Vein Disease 51 0.141
24
P HML002 Hemolytic Anemia 60 0.140
25
HDC001 Headache 52 0.138
26
MYL009 Myelodysplastic Syndrome 73 0.138
27
CRB009 Cerebritis 36 0.117
28
P ATX004 Ataxia 53 0.115
29
ADC005 Adcy5-Related Dyskinesia 11 0.114
30
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.112
31
SLP005 Sleep Disorder 52 0.109
32
NRN002 Neuronitis 40 0.109
33
P HRT032 Heart Disease 64 0.107
34
c CRN214 Coronary Heart Disease 5 22 0.103
35
P TRM003 Tremor 54 0.102
36
PRD011 Proud Syndrome 42 0.102
37
P BDD001 Budd-Chiari Syndrome 52 0.100
38
P INF032 Infertility 61 0.099
39
CHR073 Choreatic Disease 39 0.096
40
P CRN178 Coronary Heart Disease 6 22 0.094
41
ADT003 Auditory System Disease 49 0.094
42
RTN023 Retinitis 49 0.094
43
c PND001 Pain Disorder 53 0.092
44
DSS008 Disease of Mental Health 48 0.090
45
c BNG023 Benign Familial Infantile Epilepsy 40 0.090
46
EXF001 Exfoliation Syndrome 56 0.089
47
P PLN008 Peeling Skin Syndrome 45 0.089
48
STR067 Stroke, Ischemic 74 0.087
49
ATN002 Autonomic Nervous System Disease 46 0.087
50
PHY002 Physical Disorder 43 0.087
51
RSP006 Respiratory System Disease 61 0.086
52
c PLN018 Peeling Skin Syndrome 2 36 0.085
53
MTH009 Mouth Disease 63 0.085
54
DYS140 Dyskinesia, Familial, with Facial Myokymia 22 0.085
55
HYP056 Hypoglycemia 60 0.084
56
INN002 Inner Ear Disease 48 0.084
57
CNT017 Central Nervous System Origin Vertigo 27 0.084
58
WLF001 Wolff-Parkinson-White Syndrome 58 0.083
59
P HMP006 Hemiplegic Migraine 45 0.082
60
CSY001 C Syndrome 49 0.081
61
ATR060 Atrial Standstill, Digenic 51 0.081
62
P THR014 Thrombocytopenia 63 0.081
63
CHL071 Child Syndrome 58 0.080
64
KDS001 Kid Syndrome 53 0.080
65
P ESP024 Esophagitis 62 0.079
66
P PSD015 Pseudohypoparathyroidism 43 0.079
67
P HPT021 Hepatitis 74 0.079
68
PYR013 Pyruvate Kinase Deficiency 58 0.078
69
HPT074 Hepatic Adenoma, Somatic 35 0.078
70
DDN006 Duodenitis 44 0.075
71
ATH004 Athetosis 25 0.075
72
c EPS013 Episodic Kinesigenic Dyskinesia 2 9 0.074
73
ISC004 Ischemia 56 0.073
74
PRP030 Purpura 60 0.073
75
SPS057 Spasticity 41 0.073
76
c CHR096 Chronic Pulmonary Heart Disease 40 0.073
77
END072 Endotheliitis 41 0.073
78
MYC033 Myoclonus 41 0.071
79
P CRV039 Cervicitis 45 0.071
80
P PNM007 Pneumonia 67 0.071
81
P CRD011 Cardiomyopathy 66 0.070
82
P HYP086 Hypothyroidism 63 0.070
83
c THR092 Thrombophilia Due to Thrombin Defect 56 0.070
84
HPR003 Heparin-Induced Thrombocytopenia 45 0.070
85
CHL067 Cholecystitis 57 0.070
86
CHR423 Chorea, Hereditary Benign 35 0.070
87
P PNT019 Pontocerebellar Hypoplasia 39 0.070
88
WST001 West Syndrome 61 0.069
89
INS001 Insulinoma 60 0.069
90
ATN005 Autonomic Dysfunction 44 0.069
91
P SZR006 Seizure Disorder 56 0.068
92
MNR002 Meniere's Disease 49 0.067
93
SCK005 Sickle Cell Disease 51 0.067
94
HPT002 Hepatic Vein Thrombosis 38 0.067
95
ACR041 Acromelic Frontonasal Dysostosis 45 0.066
96
NSD001 Nose Disease 51 0.066
97
P MGR003 Migraine with Aura 52 0.065
98
FRN002 Frontal Lobe Epilepsy 38 0.065
99
MVD001 Moved to 60 0.063
100
PLM033 Pulmonary Embolism 59 0.063
101
BNG009 Benign Epilepsy with Centrotemporal Spikes 42 0.063
102
P MYP004 Myopathy 67 0.063
103
PRX087 Paroxysomal Nonkinesigenic Dyskinesia 3 0.063
104
P EPS003 Episodic Ataxia 58 0.062
105
c DYS119 Dystonia 9 39 0.062
106
CRB039 Cerebrovascular Disease 49 0.062
107
P HYP024 Hypoparathyroidism 52 0.062
108
P CRB042 Cerebellar Ataxia 64 0.061
109
c ART101 Aortic Valve Disease 2 56 0.061
110
P SHR029 Short Syndrome 60 0.061
111
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.061
112
P HYP265 Hypotonia 39 0.061
113
c ATM010 Autoimmune Hemolytic Anemia 59 0.059
114
PPL021 Papilledema 47 0.059
115
PTN001 Patent Foramen Ovale 55 0.059
116
P ANT006 Antiphospholipid Syndrome 60 0.059
117
WLL006 Wells Syndrome 57 0.059
118
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.059
119
GDS001 Good Syndrome 46 0.059
120
PRT018 Portal Vein Thrombosis 48 0.059
121
END074 Endocardium Disease 26 0.059
122
BRN106 Burns 52 0.059
123
P AST005 Asthma 80 0.059
124
P INT063 Intellectual Disability 46 0.059
125
P GNR027 Generalized Peeling Skin Syndrome 21 0.059
126
P CRN211 Coronary Artery Disease 74 0.059
127
CNT097 Central Hypoventilation Syndrome, Congenital 59 0.056
128
CSL001 Causalgia 42 0.056
129
P ENC004 Encephalitis 60 0.056
130
CNS004 Constipation 57 0.056
131
BRT030 Birth Defects 44 0.056
132
P BLD051 Blood Coagulation Disease 44 0.056
133
ADR009 Adrenal Cortex Disease 40 0.056
134
PRP027 Peripheral Vascular Disease 69 0.055
135
c SZR016 Seizures, Benign Familial Infantile, 2 24 0.055
136
P HMP007 Hemophilia 55 0.055
137
P LCT001 Lactic Acidosis 52 0.055
138
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.055
139
INT075 Intracranial Hypertension 52 0.055
140
THR004 Thrombocytosis 55 0.055
141
P MSC033 Muscle Disorders 52 0.055
142
HYP063 Hypersplenism 49 0.055
143
c ACT075 Acute Myocardial Infarction 61 0.055
144
P PRP034 Purpura Fulminans 41 0.055
145
SGT001 Sagittal Sinus Thrombosis 32 0.055
146
P BPL003 Bipolar Disorder 58 0.054
147
P BLP003 Blepharospasm 43 0.054
148
c PLN021 Peeling Skin Syndrome 3 30 0.054
149
c PLN017 Peeling Skin Syndrome 1 32 0.054
150
HYP005 Hypokalemia 52 0.054
151
BSL009 Basal Ganglia Calcification 41 0.052
152
P SLP006 Sleep Apnea 60 0.052
153
c CRN174 Coronary Heart Disease 2 19 0.052
154
SPS019 Spastic Paraparesis 34 0.052
155
P HLT001 Holt-Oram Syndrome 60 0.050
156
P PRC031 Preeclampsia/eclampsia 1 53 0.050
157
P INT143 Interstitial Cystitis 57 0.050
158
c ALB016 Albinism, Oculocutaneous, Type Vii 24 0.050
159
OPT006 Optic Nerve Disease 47 0.050
160
P THY054 Thyrotoxic Periodic Paralysis 46 0.050
161
P THY032 Thyroiditis 57 0.050
162
CLC006 Calcinosis 48 0.050
163
PRP028 Peripheral Vertigo 42 0.050
164
MDS022 Mediastinitis 37 0.050
165
INT010 Intracranial Embolism 32 0.050
166
c BNG076 Benign Exophthalmos Syndrome 15 0.050
167
P GNR032 Generalized Dystonia 45 0.049
168
DYS073 Dysphagia 51 0.049
169
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.049
170
MYL001 Myelitis 35 0.049
171
BLD054 Blood Protein Disease 38 0.049
172
QDR001 Quadriplegia 51 0.047
173
LKC003 Leukocyte Disease 45 0.047
174
PSY012 Psychogenic Movement 18 0.047
175
c ERL003 Early Onset Absence Epilepsy 21 0.047
176
HMD003 Hemidystonia 26 0.047
177
MSC004 Muscle Tissue Disease 35 0.047
178
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.043
179
KHL003 Kohlschutter-Tonz Syndrome 35 0.043
180
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.043
181
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.043
182
P PHT010 Photoparoxysmal Response 1 28 0.043
183
P ECL001 Eclampsia 55 0.043
184
P THR015 Thrombophilia 59 0.043
185
PLY012 Polyhydramnios 45 0.043
186
CNT025 Central Pontine Myelinolysis 43 0.043
187
NSY001 N Syndrome 42 0.043
188
c HMG003 Hemoglobin E Disease 44 0.043
189
HLL004 Hellp Syndrome 48 0.043
190
BLD053 Blood Platelet Disease 44 0.043
191
RNL097 Renal Artery Disease 44 0.043
192
CRB132 Cerebral Sinovenous Thrombosis 30 0.043
193
P PRD017 Periodic Paralyses 27 0.043
194
WLS001 Wilson Disease 72 0.042
195
RBR001 Roberts Syndrome 61 0.042
196
P ALX003 Alexander Disease 64 0.042
197
PCK002 Pick Disease 66 0.042
198
STT001 Status Epilepticus 59 0.042
199
c SZR014 Seizures, Benign Familial Infantile, 1 21 0.042
200
TRN015 Transient Cerebral Ischemia 57 0.042
201
ADJ001 Adjustment Disorder 38 0.042
202
WBR001 Weber Syndrome 36 0.042
203
CYS013 Cystinuria 63 0.035
204
c DLT002 Dilated Cardiomyopathy 75 0.035
205
c SZR007 Seizures, Benign Familial Infantile, 3 36 0.035
206
CRD119 Cardiac Arrest 63 0.035
207
c PSD066 Pseudohypoparathyroidism, Type Ib 49 0.035
208
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.035
209
ALL026 Allergic Hypersensitivity Disease 53 0.035
210
P GRV001 Graves' Disease 62 0.035
211
P MYT023 Myotonia Congenita 39 0.035
212
NRM005 Neuromuscular Disease 56 0.035
213
P BNG006 Benign Familial Neonatal Epilepsy 33 0.035
214
c CNG464 Congenital Myopathy 49 0.035
215
NWC001 Newcastle Disease 51 0.035
216
CTN007 Cutaneous Leishmaniasis 62 0.035
217
SHP003 Shapiro Syndrome 27 0.035
218
HRT011 Heart Septal Defect 40 0.035
219
HYP266 Hypoxia 55 0.035
220
IMP006 Impulse Control Disorder 40 0.035
221
CRB090 Cerebral Hypoxia 45 0.035
222
MYT011 Myotonia 40 0.035
223
CRD003 Cardiac Sarcoidosis 39 0.035
224
MND006 Mondor Disease 20 0.035